Related Products of 52415-29-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.52415-29-9, Name is 6-Bromoindole, molecular formula is C8H6BrN. In a article£¬once mentioned of 52415-29-9
Method for synthesizing 3 – (9H – xanthene -9 – yl) – 111H-indole compound by ionic liquid promoted solventless synthesis (by machine translation)
The invention discloses a method, for synthesizing 3 – (9H – xanthene -9 -yl) – 111H-indole compounds through ionic liquid promoted solventless synthesis. The target product 1 – 4h (9H – xanthene 3 – group) – 111H-indoline compound is prepared by taking an indole compound and 50 C an alcohol as a reaction substrate, and taking the betaine type hydrogen bond functionalized ionic liquid as a catalyst, and reacting -9 . The ionic liquid is simple and convenient to prepare, has good biocompatibility, is cheap and easily available; and the dosage of the ionic liquid is small, and the ionic liquid is low in dosage. Reaction conditions are mild, the atom economy is high; the reaction does not need an additional solvent, so that the use; the reaction system has no corrosivity to equipment, does not have special requirements for the reactor, and is simple. , The method is a preferred method for industrially synthesizing 3 – (9H – xanthene -9 – yl) – 111H-indole and derivatives thereof. (by machine translation)
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 52415-29-9, and how the biochemistry of the body works.Related Products of 52415-29-9
Reference£º
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles